There are 1 repository under long-read-sequencing topic.
DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.
Assembly and intrahost/low-frequency variant calling for viral samples
Graph-based assembly phasing
A pipeline for high-quality bacterial genome construction using ONT sequencing
A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.
scisorseqr is an R-package for processing of single-cell long read data and analyzing differential isoform expression across any two conditions
Single cell Nanopore sequencing data for Genotype and Phenotype
NANOME pipeline (Nanopore long-read sequencing data consensus DNA methylation detection)
Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing
A collection of publications on comparison of high-throughput sequencing technologies.
An algorithm for centromere assembly using long error-prone reads
A long-read analysis toolbox for cancer and population genomics
Fast and space-efficient taxonomic classification of long reads
A framework for extracting telomeric reads from single-molecule sequencing experiments, describing their sequence variation and motifs, and for haplotype inference.
Summarise and plot data from long-read ONT (direct RNA/cDNA) BAM files
Transcriptome long-read orientation with Deep Learning
Clair3-RNA - a long-read small variant caller for RNA sequencing data
MinION Open-source Nucleotide Identifier for Continuous Analysis - Software for MinION sequencing quantitative metagenomic analysis in real time
A collection of bioinformatics tools for use with galaxy written at Quadram Institute
Lightweight bioinformatics pipeline for microbial genome recovery
Scripts for the Nature Biotechnology paper, 2020: Automated assembly of centromeres from ultra-long error-prone reads